| | | Single nucleotide variant (3 prime UTR variant) | Hereditary persistence of fetal hemoglobin +10 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified +10 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +10 more | |
| | HBB, LOC107133510 +1 more (T124N) | Single nucleotide variant (missense variant) | not specified +10 more | |
| | HBB, LOC107133510 +1 more (E122K) | Single nucleotide variant (missense variant) | Sickle cell-Hemoglobin O Arab disease +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | not provided +10 more | |
| | | Single nucleotide variant (intron variant) | Malaria, susceptibility to +9 more | |
| | | Single nucleotide variant (intron variant) | not provided +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not provided +10 more | |
| | LOC106099062, LOC107133510 +2 more | Single nucleotide variant (splice donor variant) | Malaria, susceptibility to +11 more | |
| | HBB, LOC106099062 +1 more (T88P) | Single nucleotide variant (missense variant) | not specified +10 more | |
| | HBB, LOC106099062 +1 more (G70S) | Single nucleotide variant (missense variant) | Fetal hemoglobin quantitative trait locus 1 +11 more | GConflicting classifications of pathogenicity |
| | HBB, LOC106099062 +1 more (L69F) | Single nucleotide variant (missense variant) | not provided +9 more | GPathogenic/Likely pathogenic |
| | HBB, LOC106099062 +1 more (V68fs) | Deletion (frameshift variant) | not provided +10 more | |
| | HBB, LOC106099062 +1 more (K62*) | Single nucleotide variant (nonsense) | beta Thalassemia +10 more | |
| | LOC106099062, LOC107133510 +1 more (G57S) | Single nucleotide variant (missense variant) | not provided +10 more | |
| | LOC107133510, HBB +1 more (F46fs) | Deletion (frameshift variant) | not provided +10 more | GPathogenic/Likely pathogenic |
| | HBB, LOC106099062 +1 more (F42fs) | Deletion (frameshift variant) | not provided +13 more | GPathogenic/Likely pathogenic |
| | HBB, LOC106099062 +1 more (R41S) | Single nucleotide variant (missense variant) | Erythrocytosis, familial, 6 +9 more | |
| | HBB, LOC106099062 +1 more (Q40*) | Single nucleotide variant (nonsense) | Malaria, susceptibility to +12 more | |
| | HBB, LOC106099062 +1 more (W38fs) | Deletion (frameshift variant) | Hemoglobinopathy +11 more | |
| | | Single nucleotide variant (intron variant) | Malaria, susceptibility to +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Malaria, susceptibility to +12 more | GConflicting classifications of pathogenicity |
| | LOC106099062, LOC107133510 +1 more | Single nucleotide variant (intron variant) | Malaria, susceptibility to +13 more | |
| | | Single nucleotide variant (splice donor variant) | not provided +10 more | |
| | LOC106099062, LOC107133510 +1 more | Single nucleotide variant (splice donor variant) | not provided +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | not provided +11 more | |
| | HBB, LOC106099062 +1 more (E27K) | Single nucleotide variant (missense variant) | Malaria, susceptibility to +15 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +10 more | GPathogenic/Likely pathogenic |
| | HBB, LOC106099062 +1 more (E23V) | Single nucleotide variant (missense variant) | not provided +9 more | |
| | HBB, LOC106099062 +1 more (V21M) | Single nucleotide variant (missense variant) | Hereditary persistence of fetal hemoglobin +9 more | |
| | HBB, LOC106099062 +1 more (K18*) | Single nucleotide variant (nonsense) | not provided +10 more | |
| | HBB, LOC106099062 +1 more (K18fs) | Deletion (frameshift variant) | Hemoglobinopathy +13 more | |
| | HBB, LOC106099062 +1 more (L15P) | Single nucleotide variant (missense variant) | not specified +10 more | |
| | HBB, LOC106099062 +1 more (V12I) | Single nucleotide variant (missense variant) | Hb SS disease +13 more | |
| | HBB, LOC106099062 +1 more (S10fs) | Duplication (frameshift variant) | Malaria, susceptibility to +11 more | GConflicting classifications of pathogenicity |
| | HBB, LOC106099062 +1 more (E7fs) | Deletion (frameshift variant) | not provided +10 more | |
| | LOC106099062, LOC107133510 +1 more (E7V) | Single nucleotide variant (missense variant) | Malaria, susceptibility to +15 more | |
| | HBB, LOC106099062 +1 more (E7K) | Single nucleotide variant (missense variant) | HBB-related disorder +15 more | |
| | LOC106099062, LOC107133510 +1 more (P6fs) | Deletion (frameshift variant) | HBB-related disorder +11 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +14 more | |
| | | Single nucleotide variant | beta Thalassemia +10 more | |
| | | Single nucleotide variant | not provided +11 more | |
| | | Single nucleotide variant | not specified +10 more | |
| | | Single nucleotide variant | not provided +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant | Beta thalassemia intermedia +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant | Hemoglobinopathy +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant | Malaria, susceptibility to +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant | not provided +9 more | |